Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview01:32

Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview

3.5K
Cyanohydrins are compounds that contain –CN and –OH groups on the same carbon atom. They are formed by the nucleophilic addition of the cyanide ions to the carbonyl group. Cyanide ions are highly basic and nucleophilic and can be generated from HCN under aqueous conditions. However, since HCN is a weak acid, the number of cyanide ions generated is very small. Hence, a small amount of base or KCN/NaCN is added to HCN to increase the concentration of the cyanide ions in the reaction...
3.5K
Hydrolysis of Chlorobenzene to Phenol: Dow Process01:10

Hydrolysis of Chlorobenzene to Phenol: Dow Process

3.5K
Simple aryl halides do not react with nucleophiles under normal conditions. However, the reaction can proceed under drastic conditions involving high temperatures and high pressure to give the substituted products. For example, chlorobenzene is converted to phenol using aqueous sodium hydroxide at 350 °C under high pressure by the Dow process. The reaction follows an elimination-addition mechanism involving a benzyne intermediate. Here, the chloride ion is...
3.5K
Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism01:10

Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism

3.8K
Cyanohydrins are formed when cyanide nucleophiles and carbonyl compounds like aldehydes and ketones react. A strong base, the cyanide ion, catalyzes cyanohydrin formation. The ions are generated from HCN under aqueous conditions. Once the cyanide ions are generated, the first step involves the nucleophilic attack of the cyanide ions on the electrophilic carbonyl carbon. This attack shifts the π electrons from the C=O to the oxygen atom forming the alkoxide ion intermediate. The alkoxide anion...
3.8K
Hydrolysis01:15

Hydrolysis

119.5K
Overview
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...
119.5K
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration02:40

Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration

9.6K
Introduction
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
9.6K
Hydrolysis of ATP01:08

Hydrolysis of ATP

79.6K
The bonds of adenosine triphosphate (ATP) can be broken through the addition of water, releasing one or two phosphate groups in an exergonic process called hydrolysis. This reaction liberates the energy in the bonds for use in the cell—for instance, to synthesize proteins from amino acids.
If one phosphate group is removed, a molecule of ADP—adenosine diphosphate—remains, along with inorganic phosphate. ADP can be further hydrolyzed to AMP—adenosine...
79.6K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Whole Exome Sequencing as a Diagnostic Tool for Complex Neurological Disorders.

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research·2016
Same author

13-cis-retinoic acid affects oxidation and DNA damage in oxidative-positive SLE lymphocytes but may not be useful for therapy.

Biochemical medicine and metabolic biology·1993
Same author

Correlation of perinatal brain growth with age, body size, sex, and race.

Journal of neuropathology and experimental neurology·1986
Same author

The weight of the infratentorial portion of the adult brain and analysis of the infratentorial/whole brain weight ratio.

Journal of neuropathology and experimental neurology·1982
Same author

Newborn brain weight in relation to maturity, sex, and race.

Annals of neurology·1981
Same author

Analysis of brain weight. I. Adult brain weight in relation to sex, race, and age.

Archives of pathology & laboratory medicine·1980
Same journal

What the American Medical Association Thinks of the Electronic Reactions of Abrams.

The Dental register·2021
Same journal

A Few Remarks on the Role of the American Dentists in Paris during the Great War.

The Dental register·2021
Same journal

Event and Comment.

The Dental register·2021
Same journal

A Message from Thwaites.

The Dental register·2021
Same journal

Cuspid Relationship and Pyorrhea Alveolaris.

The Dental register·2021
Same journal

Defective Teeth and Nutrition.

The Dental register·2021
See all related articles

Related Experiment Video

Updated: Nov 14, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
12:07

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes

Published on: April 1, 2013

17.4K

Hydronaphthol

G Monroe

    The Dental Register
    |March 11, 2021
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
    12:27

    Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes

    Published on: September 8, 2013

    11.1K
    Hydrophobic Salt-modified Nafion for Enzyme Immobilization and Stabilization
    11:16

    Hydrophobic Salt-modified Nafion for Enzyme Immobilization and Stabilization

    Published on: July 11, 2012

    16.5K

    Related Experiment Videos

    Last Updated: Nov 14, 2025

    Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
    12:07

    Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes

    Published on: April 1, 2013

    17.4K
    Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
    12:27

    Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes

    Published on: September 8, 2013

    11.1K
    Hydrophobic Salt-modified Nafion for Enzyme Immobilization and Stabilization
    11:16

    Hydrophobic Salt-modified Nafion for Enzyme Immobilization and Stabilization

    Published on: July 11, 2012

    16.5K